Existing Research Sites
NCR provides trial management, site support, training, regulatory submissions, and helps secure new trials for qualified physicians.
Help in site feasibilities
Full Coordinator support for the duration of the study
Training at reasonable cost
ICH/GCP trainings for Coordinators and Principal Investigators
Source document preparations/ Contract and budget negotiations
Help in Sponsor/FDA Audits
Regulatory document preparations and submissions on your behalf
We help you getting new trials to your site for your qualified physicians
Offer back up coordinator services for your primary coordinators
IRB submission
Regulatory Document submissions
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